The thrombomodulin gene mutation G127→A (Ala25Thr) and cerebrovascular disease

Cerebrovascular Diseases

Volumn 10, Issue 5, 2000, Pages 359-363

  Warner, Darren ^a   Catto, Andrew ^a   Kunz, Gabriella ^b   Ireland, Helen ^b   Grant, Peter J ^a   Lane, David A ^b  

^a LEEDS GENERAL INFIRMARY   (United Kingdom)

^b IMPERIAL COLLEGE SCHOOL OF MEDICINE   (United Kingdom)

Author keywords

Genetics; Mutation; Risk factors; Thrombomodulin

Indexed keywords

THROMBOMODULIN;

ADULT; AGED; ARTICLE; CEREBROVASCULAR DISEASE; CONTROLLED STUDY; DNA DETERMINATION; FEMALE; GENE AMPLIFICATION; GENE FREQUENCY; HUMAN; MAJOR CLINICAL STUDY; MALE; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; STROKE;

AGED; AGED, 80 AND OVER; CEREBROVASCULAR DISORDERS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; POINT MUTATION; RISK FACTORS; THROMBOMODULIN;

EID: 0033818717     PISSN: 10159770     EISSN: None     Source Type: Journal    
DOI: 10.1159/000016091     Document Type: Article

References (27)